The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
63201792 6320179 2 F 20160831 20070525 20160902 EXP GB-BRISTOL-MYERS SQUIBB COMPANY-13790696 BRISTOL MYERS SQUIBB 0.00 N Y 0.00000 20160902 CN GB GB

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
63201792 6320179 1 PS CAPTOPRIL. CAPTOPRIL 1 Transplacental 25 MG, BID U U 0 25 MG TABLET BID
63201792 6320179 2 C BECLOFORTE 2 Transplacental UNK U U 0
63201792 6320179 3 C BRICANYL TERBUTALINE SULFATE 1 Transplacental UNK U U 0
63201792 6320179 4 C THYROXINE LEVOTHYROXINE 1 Transplacental 100 ?G, QD U U 0 100 UG QD
63201792 6320179 5 C VOLMAX ALBUTEROL SULFATE 1 Transplacental 8 MG, BID U U 0 8 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
63201792 6320179 1 Product used for unknown indication
63201792 6320179 2 Product used for unknown indication
63201792 6320179 3 Product used for unknown indication
63201792 6320179 4 Product used for unknown indication
63201792 6320179 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
63201792 6320179 OT
63201792 6320179 DE
63201792 6320179 CA

Reactions reported

Event ID CASEID DRUG REC ACT PT
63201792 6320179 Foetal exposure during pregnancy
63201792 6320179 Hypoplastic left heart syndrome

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
63201792 6320179 1 19890610 19920302 0
63201792 6320179 2 19891006 0
63201792 6320179 3 19891006 0
63201792 6320179 4 19891006 0
63201792 6320179 5 19891006 0